Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3010221586

FEI Number

3010221586

Entity Name

Thunderbird Molding Greensboro

City/State/Country

Greensboro, NC, US

Establishment Address

4833 W Gate City Blvd, Greensboro, NC 27407, US

Establishment Type(s)

Manufacture Medical Device for Another Party (Contract Manufacturer)

Owner / Operator

Thunderbird Manufacturing LLC (Owner Number: 10086859)

Owner / Operator Contact Address

900 Commerce Dr, Suite 150, Oak Brook, IL 60523, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

550 553 CLR Irragator 556 Preemie Pouch Preemie Pouch Port Neutra Skin CLR Port; CLR Port Cap; CLR Port Injector Rehrig Healthcare

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
HTD	Forceps	General, Plastic Surgery	Class 1	878.4800	2022-12-16
GCX	Apparatus, Suction, Operating-Room, Wall Vacuum Powered	General Hospital	Class 2	880.6740	2022-12-16
HFW	Clamp, Umbilical	Obstetrics/Gynecology	Class 2	884.4530	2022-12-16
FON	Bag, Drainage, With Adhesive, Ostomy	Gastroenterology, Urology	Class 1	876.5900	2022-12-16
GCE	Adaptor, Catheter	General, Plastic Surgery	Class 1	878.4200	2022-12-16
MMK	Container, Sharps	General Hospital	Class 2	880.5570	2022-12-16

Official Correspondent

Joseph Vest

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Thunderbird Manufacturing LLC

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

Related 510(k) Records

510(k) Number	Applicant	Device Name	Decision Date
K852723	The Huxley Instrument Corp.	FOERSTER SPONGE FORCEPS, SERRATED, 7+SS 410 OR 420	1985-07-15
K873512	Arthropedics, Inc.	SERRATED GRASPING FORCEPS, RIGHT	1987-11-02

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3010287737	BAECHLER FEINTECH AG	Hoelstein Basel-Landschaft, CH
3003675041	SURGICAL INSTRUMENTS BELGIUM SA	GEMBLOUX Namur, BE

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3010221586. Last updated year: 2026. Please use registration number 3010221586 when referencing this establishment in official correspondence.